Canonical Allele Identifier: CA2351374482

Gene: NDUFAF5

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.13801794_13801795delinsTC , CM000682.2:g.13801794_13801795delinsTC	GRCh38
NC_000020.10:g.13782440_13782441delinsTC , CM000682.1:g.13782440_13782441delinsTC	GRCh37
NC_000020.9:g.13730440_13730441delinsTC	NCBI36
NG_015811.1:g.21769_21770delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378106.10:c.717+111_717+112delinsTC MANE Select	ENSP00000367346.5:n.717+111_717+112delinsTC
ENST00000378081.9:c.717+111_717+112delinsTC	ENSP00000437325.1:n.717+111_717+112delinsTC
ENST00000378106.9:c.717+111_717+112delinsTC	ENSP00000367346.5:n.717+111_717+112delinsTC
ENST00000463598.1:c.633+111_633+112delinsTC	ENSP00000420497.1:n.633+111_633+112delinsTC
ENST00000464269.5:n.390+111_390+112delinsTC
ENST00000475968.5:n.594+111_594+112delinsTC
ENST00000476124.1:n.117-24_117-23delinsTC
ENST00000476536.5:n.677+111_677+112delinsTC
ENST00000477732.5:n.502+3294_502+3295delinsTC
ENST00000479716.5:n.238+111_238+112delinsTC
ENST00000481249.5:n.594+111_594+112delinsTC
ENST00000485738.5:n.694+111_694+112delinsTC
ENST00000487478.5:n.142-24_142-23delinsTC
NM_001039375.2:c.633+111_633+112delinsTC	NP_001034464.1:n.633+111_633+112delinsTC
NM_024120.4:c.717+111_717+112delinsTC	NP_077025.2:n.717+111_717+112delinsTC
NR_029377.1:n.760+111_760+112delinsTC
XM_006723620.2:c.718-24_718-23delinsTC	XP_006723683.1:n.718-24_718-23delinsTC
XM_006723622.2:c.246+111_246+112delinsTC	XP_006723685.1:n.246+111_246+112delinsTC
XM_006723623.1:c.246+111_246+112delinsTC	XP_006723686.1:n.246+111_246+112delinsTC
XM_006723624.1:c.246+111_246+112delinsTC	XP_006723687.1:n.246+111_246+112delinsTC
XM_011529341.1:c.717+111_717+112delinsTC	XP_011527643.1:n.717+111_717+112delinsTC
XM_011529342.1:c.717+111_717+112delinsTC	XP_011527644.1:n.717+111_717+112delinsTC
XM_011529343.1:c.717+111_717+112delinsTC	XP_011527645.1:n.717+111_717+112delinsTC
XM_011529344.1:c.348+111_348+112delinsTC	XP_011527646.1:n.348+111_348+112delinsTC
XR_430269.2:n.738-24_738-23delinsTC
XR_937140.1:n.737+111_737+112delinsTC
NM_001352403.1:c.246+111_246+112delinsTC	NP_001339332.1:n.246+111_246+112delinsTC
NM_001352406.1:c.156+111_156+112delinsTC	NP_001339335.1:n.156+111_156+112delinsTC
NM_001352407.1:c.156+111_156+112delinsTC	NP_001339336.1:n.156+111_156+112delinsTC
NM_001352408.1:c.718-24_718-23delinsTC	NP_001339337.1:n.718-24_718-23delinsTC
NR_147978.1:n.761-24_761-23delinsTC
NR_147979.1:n.780+111_780+112delinsTC
NR_147980.1:n.656+111_656+112delinsTC
NR_147981.1:n.894+111_894+112delinsTC
NR_147982.1:n.895-24_895-23delinsTC
NR_147983.1:n.810+111_810+112delinsTC
XM_006723624.2:c.246+111_246+112delinsTC	XP_006723687.1:n.246+111_246+112delinsTC
XM_011529342.2:c.717+111_717+112delinsTC	XP_011527644.1:n.717+111_717+112delinsTC
XM_024451999.1:c.246+111_246+112delinsTC	XP_024307767.1:n.246+111_246+112delinsTC
XR_001754396.1:n.676+111_676+112delinsTC
XR_430269.3:n.738-24_738-23delinsTC
XR_937140.2:n.737+111_737+112delinsTC
NM_024120.5:c.717+111_717+112delinsTC MANE Select	NP_077025.2:n.717+111_717+112delinsTC
NM_001039375.3:c.633+111_633+112delinsTC	NP_001034464.1:n.633+111_633+112delinsTC
NM_001352403.2:c.246+111_246+112delinsTC	NP_001339332.1:n.246+111_246+112delinsTC
NM_001352406.2:c.156+111_156+112delinsTC	NP_001339335.1:n.156+111_156+112delinsTC
NM_001352407.2:c.156+111_156+112delinsTC	NP_001339336.1:n.156+111_156+112delinsTC
NR_029377.2:n.758+111_758+112delinsTC
NR_147978.2:n.759-24_759-23delinsTC
NR_147979.2:n.778+111_778+112delinsTC
NR_147980.2:n.654+111_654+112delinsTC
NR_147981.2:n.892+111_892+112delinsTC
NR_147982.2:n.893-24_893-23delinsTC
NR_147983.2:n.808+111_808+112delinsTC
NM_001352408.2:c.718-24_718-23delinsTC	NP_001339337.1:n.718-24_718-23delinsTC